A combined advanced oxidation process based on the electrochemical oxidation of chloramphenicol (CHL) on a boron-doped diamond (BDD) electrode under UV irradiation was investigated. The influence of the main process parameters (current density, pH, temperature, and chloride concentration) on CHL degradation and mineralization was assessed. An estimation of the energy consumption required to mineralize CHL was also made. The results showed that CHL can be completely degraded and extensively mineralized by 3-h UV-assisted anodic oxidation on BDD. The process can be further accelerated by chlorides, as these species act as precursors for the photo-induced formation of radical species contributing to CHL oxidation. Under optimal conditions (300 mA m–2, 0.01 M NaCl, ambient temperature, and pH 10), complete CHL removal occurred after 150 min of treatment, and approximately 95 % mineralization was achieved in 180 min. Overall, the results obtained suggest that the investigated process may represent a promising approach to treat wastewaters containing CHL or other recalcitrant antibiotics.
Degradation of chloramphenicol in water by oxidation on a boron-doped diamond electrode under UV irradiation / Ennouri, R.; Lavecchia, R.; Zuorro, A.; Elaoud, S. C.; Petrucci, E.. - In: JOURNAL OF WATER PROCESS ENGINEERING. - ISSN 2214-7144. - 41:(2021). [10.1016/j.jwpe.2021.101995]
Degradation of chloramphenicol in water by oxidation on a boron-doped diamond electrode under UV irradiation
Lavecchia R.;Zuorro A.
;Petrucci E.Ultimo
2021
Abstract
A combined advanced oxidation process based on the electrochemical oxidation of chloramphenicol (CHL) on a boron-doped diamond (BDD) electrode under UV irradiation was investigated. The influence of the main process parameters (current density, pH, temperature, and chloride concentration) on CHL degradation and mineralization was assessed. An estimation of the energy consumption required to mineralize CHL was also made. The results showed that CHL can be completely degraded and extensively mineralized by 3-h UV-assisted anodic oxidation on BDD. The process can be further accelerated by chlorides, as these species act as precursors for the photo-induced formation of radical species contributing to CHL oxidation. Under optimal conditions (300 mA m–2, 0.01 M NaCl, ambient temperature, and pH 10), complete CHL removal occurred after 150 min of treatment, and approximately 95 % mineralization was achieved in 180 min. Overall, the results obtained suggest that the investigated process may represent a promising approach to treat wastewaters containing CHL or other recalcitrant antibiotics.File | Dimensione | Formato | |
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